| “A study in yellow”: Investigations in the stereoselectivity of ene‐reductases F Parmeggiani, E Brenna, D Colombo, FG Gatti, F Tentori, D Tessaro ChemBioChem 23 (1), e202100445, 2022 | 45 | 2022 |
| Conversion of oleic acid into azelaic and pelargonic acid by a chemo-enzymatic route E Brenna, D Colombo, G Di Lecce, FG Gatti, MC Ghezzi, F Tentori, ... Molecules 25 (8), 1882, 2020 | 36 | 2020 |
| Bioprocess Intensification Using Flow Reactors: Stereoselective Oxidation of Achiral 1,3-diols with Immobilized Acetobacter Aceti V De Vitis, F Dall’Oglio, F Tentori, ML Contente, D Romano, E Brenna, ... Catalysts 9 (3), 208, 2019 | 33 | 2019 |
| Biocatalytic synthesis of chiral cyclic γ-oxoesters by sequential C–H hydroxylation, alcohol oxidation and alkene reduction E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, A Pugliese, ... Green Chemistry 19 (21), 5122-5130, 2017 | 33 | 2017 |
| Enzymatic methods for the manipulation and valorization of soapstock from vegetable oil refining processes B Casali, E Brenna, F Parmeggiani, D Tessaro, F Tentori Sustainable Chemistry 2 (1), 74-91, 2021 | 27 | 2021 |
| Immobilization of old yellow enzymes via covalent or coordination bonds F Tentori, T Bavaro, E Brenna, D Colombo, D Monti, R Semproli, D Ubiali Catalysts 10 (2), 260, 2020 | 22 | 2020 |
| Biocatalytic approach to chiral β-nitroalcohols by enantioselective alcohol dehydrogenase-mediated reduction of α-nitroketones F Tentori, E Brenna, D Colombo, M Crotti, FG Gatti, MC Ghezzi, ... Catalysts 8 (8), 308, 2018 | 19 | 2018 |
| Ene-reductase transformation of massoia lactone to δ-decalactone in a continuous-flow reactor E Szczepańska, D Colombo, F Tentori, T Olejniczak, E Brenna, D Monti, ... Scientific Reports 11 (1), 18794, 2021 | 16 | 2021 |
| Continuous-flow biocatalytic process for the synthesis of the best stereoisomers of the commercial fragrances leather cyclohexanol (4-isopropylcyclohexanol) and woody acetate … F Tentori, E Brenna, M Crotti, G Pedrocchi-Fantoni, MC Ghezzi, D Tessaro Catalysts 10 (1), 102, 2020 | 14 | 2020 |
| Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2‐Alkynals/3‐Alkyn‐2‐ones into 4‐Alkynals/Alkynols D Colombo, E Brenna, FG Gatti, MC Ghezzi, D Monti, F Parmeggiani, ... Advanced Synthesis & Catalysis 361 (11), 2638-2648, 2019 | 12 | 2019 |
| Multi-step chemo-enzymatic synthesis of azelaic and pelargonic acids from the soapstock of high-oleic sunflower oil refinement B Casali, E Brenna, F Parmeggiani, F Tentori, D Tessaro Green Chemistry 24 (5), 2082-2093, 2022 | 11 | 2022 |
| Lipase-mediated synthesis of oleoyl ethanolamide starting from high-oleic sunflower oil soapstock E Brenna, V De Fabritiis, F Parmeggiani, F Tentori, D Tessaro ACS Sustainable Chemistry & Engineering 11 (7), 2764-2772, 2023 | 4 | 2023 |
| Oxidation of threo‐9,10‐Dihydroxystearic Acid Mediated by Micrococcus luteus as a Key Step in the Conversion of Oleic Acid into Pelargonic and Azelaic Acids D Colombo, E Brenna, B Casali, MC Ghezzi, F Parmeggiani, F Tentori, ... ChemCatChem 13 (14), 3275-3282, 2021 | 4 | 2021 |
| Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal F Tentori, E Brenna, C Ferrari, FG Gatti, MC Ghezzi, F Parmeggiani Reaction Chemistry & Engineering 6 (9), 1591-1600, 2021 | 2 | 2021 |
| Development of a flow process for an easy and fast access to 2-pyrone derivatives GIC Righetti, F Tentori, E Brenna, C Gambarotti Reaction Chemistry & Engineering 8 (1), 199-204, 2023 | | 2023 |
| Synthesis of biologically active molecules by continuous flow biocatalysis F Tentori | | 2021 |
| Enantioselective desymmetrisation of achiral 2-substituted-1, 3-diols by acetobacter aceti: traditional approach and developments F TENTORI Politecnico di Milano, 2015 | | 2015 |
| Ene-Reductases for Organic Synthesis Applications: Chemoselective Hydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2-Alkynals into 4-Alkynals/Alkynols D Colombo, E Brenna, FG Gatti, MC Ghezzi, D Monti, F Parmeggiani, ... | | |
| Multi-step chemo-enzymatic synthesis of azelaic and pelargonic acids from the soapstock of high-oleic sunflower oil refinement F Tentori, E Brenna, B Casali, F Parmeggiani, D Tessaro Synthesis of biologically active molecules by continuous flow biocatalysis, 137, 0 | | |
